Suppliers / Livzon Group Ningxia Pharmaceutical

Livzon Group Ningxia Pharmaceutical

China 2 duplicate records merged Updated 9 July 2026

Livzon Group Ningxia Pharmaceutical is an API manufacturer based in China. It holds 3 active US drug master files across a filed portfolio of 3 molecules.

3
active US DMFs
0
valid CEPs
0
registered plants
6
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Lovastatin US FDA 1
Mevastatin US FDA 1
Mycophenolic Acid US FDA 1

Also appears on these molecule pages

Lovastatin API Mycophenolic Acid API

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 6 None

Questions about Livzon Group Ningxia Pharmaceutical

Does Livzon Group Ningxia Pharmaceutical hold a US DMF or a CEP?
Livzon Group Ningxia Pharmaceutical holds 3 active US drug master files. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
What does Livzon Group Ningxia Pharmaceutical make?
3 molecules are on record against Livzon Group Ningxia Pharmaceutical, including Lovastatin, Mevastatin and Mycophenolic Acid. Each links through to that molecule's full manufacturer list.
Where does Livzon Group Ningxia Pharmaceutical file?
Filings are on record with DAV (Vietnam), 6 in total.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability